Once a project has been approved by an IRB, researchers must adhere
to the approved protocol and follow anyadditional IRB instructions.
This, unfortunately, is where a few researchers and institutions have
occasionally run into problems and temporarily had their “assurance”
(FWA - Federalwide Assurance) suspended. The continuing responsibilities
that researchers have include:
- enrolling only those subjects that meet IRB approvedinclusion and
exclusion criteria,
- properly obtaining and documenting informed consent,
- obtaining prior approval for any deviation from theapproved protocol,
- keeping accurate records, and
- promptly reporting to the IRB any unanticipated problems involving
risks to subjects or others.
While research institutions are increasingly monitoringthe progress
of human subjects research, the primary responsibility for conducting
experiments as approved still lies with the individual researchers and
staff who conduct the experiments.